Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555395486
rs1555395486
G 0.700 CausalMutation CLINVAR Performant Mutation Identification Using Targeted Next-Generation Sequencing of 14 Thoracic Aortic Aneurysm Genes. 25907466

2015

dbSNP: rs1555395486
rs1555395486
G 0.700 CausalMutation CLINVAR Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study. 17701892

2007

dbSNP: rs1555395486
rs1555395486
G 0.700 CausalMutation CLINVAR The molecular genetics of Marfan syndrome and related disorders. 16571647

2006

dbSNP: rs1555395486
rs1555395486
G 0.700 CausalMutation CLINVAR Fibrillin-1 misfolding and disease. 16677079

2006

dbSNP: rs1555395486
rs1555395486
G 0.700 CausalMutation CLINVAR Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders. 10464652

1999

dbSNP: rs1555395486
rs1555395486
G 0.700 CausalMutation CLINVAR Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1: distinct effects on biochemical and clinical phenotypes. 10486319

1999

dbSNP: rs1555395486
rs1555395486
G 0.700 CausalMutation CLINVAR The solution structure of human epidermal growth factor. 3495735

1987

dbSNP: rs1555395486
rs1555395486
G 0.700 CausalMutation CLINVAR Epidermal growth factor. Location of disulfide bonds. 4750422

1973

dbSNP: rs1555395486
rs1555395486
G 0.700 GeneticVariation CLINVAR